OPERATING AND MAINTENANCE MANUAL

- CONTINUOUS VACUUM REGULATORS DIGITAL & ANALOG

Vacuum Regulator Type:

Body Colors:

VR - XX Y Y - XX Y Z Display:

Color Code:

Wall Connection:

Patient Connection:

Basic matrix shown. Consult the Amvex Catalogue for full matrix or contact your Amvex representative.

Rx ONLY

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25B East Pearce St., Richmond Hill, ON L4B 2M9 Canada | Tel: 905.764.7736 | Fax: 905.764.7743 | www.amvex.com

®

1111 Lakeside Drive, Gurnee, IL 60031-4099 | Tel: 1.800.448.0770 | Fax: 847.855.6300 www.ohiomedical.com 1

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2 Mode Face Assembly 3 Mode Face Assembly

1

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2. Analog Lens 0-100mmHg Gauge (Analog or Digital) 0-160mmHg Gauge (Analog or Digital) 3. Gauge 0-200mmHg Gauge (Analog or Digital) 0-300mmHg Gauge (Analog or Digital) 0-760mmHg Gauge (Analog or Digital) 4. Gauge O-rings (2pcs) 5. Selector Screw 2 Mode Continuous 6. Selector Face Plate 3 Mode Continuous 7. Selector Switch O-ring 8. Selector Gasket 9. Index ball 10. Index Spring 11. Back Body 12. Selector Plug 13. Selector Plug O-ring 14. Back Gasket 15. Back Plate 3 16. Cover Screws ( 4 pcs) 2 17. Back Plate Screws (2 pcs) 18. Bottom Plate Screw

1. Face Assembly

5

19

9

25 26 20 24

23 s) 4 (2 pcs)

7

8

21

E

10

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F

G

H

22 (2 pcs)

11

12 13

I

Positive Pressure Relief Valve Port Cap (2 pcs) Pediatric Relief Screw Pediatric Relief Body Pediatric & Neonatal Pediatric Relief Ball Models only Pediatric Relief O-ring 14

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21. 22. 23. 24. 25. 26.

A (2pcs)

B

C

D

K

17

18

16

16

16

17

16

E. Diaphragm F. Support Plate G S

Regulating Module Parts List: A. Cap Screws (2pcs) G. Regulating Spring ReRegulating gulating MoCap dule B. H. Stem C. Stem Screw I. Regulating Body A. Cap Screws (2 pc D. Top Plate J. Body O-rings (2 pcs) B. Regulating Cap E. K. Stem O-ring C. Diaphragm Stem Screw D.Support Top PlatePlate F.

J(2pcs.)

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Standard, Pediatric & Neonatal Regulating Module High Regulating Module

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19. Orifice 20. Regulating Module

CONTINUOUS VACUUM REGULATOR PART IDENTIFICATION

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IMPORTANT: SAFETY INSTRUCTIONS This manual provides you with important information about the Vacuum Regulators and should be read carefully to ensure the safe and proper use of this product. Read and understand all the safety and operating instructions contained in this booklet. If you do not understand these instructions, or have any questions, contact your supervisor, dealer or the manufacturer before attempting to use the apparatus.

! WARNING: ATTENTION: CAUTION:

! 0413

Indicates a potentially hazardous situation, which if not avoided, could result in death or serious injury. Indicates a potentially hazardous situation, which if not avoided, could result in minor or moderate injury. Indicates a potentially hazardous situation, which if not avoided, could result in damage to the device or other property. Consult operating manual. Symbol indicates the device complies with the requirements of Directive 93/42/EEC concerning medical devices (on CE marked devices only).

Receiving Inspection Remove product from package and inspect for damage. If product is damaged, DO NOT USE and contact your dealer or equipment provider. ATTENTION:

It is very important to allow product to remain in original packaging for 12-24 hours to acclimate to room temperature before use

User Responsibility ! WARNING:

This device is to be used ONLY by people who have been properly trained on the operation of the device. Operation of this device is not to be done if flammable anesthetics are present due to the possibility of explosion caused by static charge.

This product performs as explained in this manual as long as the assembly, use, repair and maintenance are properly followed according to our instructions. Periodic review of this device is recommended. If any damage or defects are present, the product should not be used. This includes parts that may have been altered, contaminated, worn or missing. If any of the above are noted, immediate repair / replacement is required. In compliance with the Amvex Warranty, repair of this device is not to be performed by anyone other than a qualified professional. If this device is subject to improper maintenance, repair, use and/or abuse leading to malfunction of the device, replacement is the sole responsibility of the user. ATTENTION:

Service of this device should ONLY be performed by properly trained individuals. This product contains magnetic, ferrous material that may affect the

MRI WARNING: result of an MRI. MR Conditional options may be available, contact your

Amvex sales representative at 1-866-462-6839 or 905-764-7736.

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Vacuum Regulator Model

Gauge Range

Gauge Accuracy Analog

Digital

0 - 200 mmHg

+/- 3% F.S.

+/- 1% F.S. at 22ºC

0 - 300 mmHg

+/- 3% F.S.

+/- 1% F.S. at 22ºC

Pediatric Continuous / Intermittent

0 - 160 mmHg

+/- 3% F.S.

+/- 1% F.S. at 22ºC

Neonatal Continuous / Intermittent

0 - 100 mmHg

+/- 3% F.S.

+/- 1% F.S. at 22ºC

High

0 - 760 mmHg

+/- 3% F.S.

+/- 1% F.S. at 22ºC

Continuous / Intermittent

Please note: F.S. = Full Scale

Flow Rates Continuous

Standard

Pediatric

0 - 80 LPM

0 - 40 LPM

Intended Use Amvex Vacuum Regulators are intended to regulate a supplied vacuum pressure to the user’s desired vacuum level. A gauge shows the value of the regulated vacuum, which is adjustable via a regulating knob.

Operating Instructions ATTENTION:

The operating and storage temperature for the regulator should reflect typical environmental conditions of a medical facility environment. DO NOT attempt to change, alter or modify the intended use of the product.

Equipment Setup: Depending on the desired location of the regulator, connect the vacuum adapter directly into the wall outlet, or connect one end of an Amvex Corporation vacuum hose assembly onto the supply port of the suction regulator and the other end onto the vacuum source (i.e. wall outlet). Suction tubing, provided by the hospital, is required between the patient and patient port of the canister, as well as between the outlet port of the Vacuum Regulator and canister. 1/4” connection tubing is recommended by NFPA®.* To prevent possible contamination of the regulator, a high flow suction filter or an overflow safety trap provided by Amvex is recommended between the regulator and the collection canister. NFPA recommends use of an overflow trap to protect the vacuum regulator outlet and vacuum system. *National Fire Protection Association (NFPA 99-2002). Healthcare facilities pages 497-498.

Selecting the Mode: REG: OFF: FULL:

NOTE:

Allows degree of vacuum to be adjusted by use of the regulating knob. Vacuum is no longer on or being supplied to patient. Maximum vacuum is administered to patient. FULL mode is only available on the 3 mode models 4

Battery Low Indicator: NOTE: When a battery icon appears on the gauge it indicates that the battery is low. Please take the unit out of service immediately and contact an Amvex/Ohio Medical Customer Service Representative for battery replacement. If the low battery condition is not addressed and the battery becomes fully depleted, the gauge will not show any readout including the low battery icon or gauge pressure. If the gauge were to go blank during suctioning, the unit will continue to suction and the intermittent feature will continue to operate. Once completing that procedure, It is important to immediately take the unit out of service and contact Amvex/Ohio Medical Customer Service Representative for battery replacement.

Procedures Prior to Use List: ! WARNING: The following tests are recommended prior to use on each patient. If the Vacuum Regulator does not pass one or more of the following tests outlined on the checklist it should be evaluated, repaired and/or replaced by a qualified individual. The following tests must be done with a minimum supply vacuum of -53 kPa(-400 mmHg):

1. Move the selector switch to the “OFF” position. Turn the regulator knob one complete turn in the clockwise direction. Kink the vacuum tubing to block the outlet. There should be no movement of the gauge needle (or in case of a digital gauge, no change in display). 2. Move the selector switch to the “REG” position. Turn the regulator knob fully in the counter-clockwise direction. Kink the vacuum tubing; again, there should be no movement of the gauge needle (or in case of a digital gauge, no change in display). 3. Kink vacuum tubing. Regulator Setting: Standard: Increase the vacuum to -12 kPa (-90 mmHg) Pediatric & Neonatal: Increase the vacuum to -5 kPa (-40 mmHg) 4. Open and close the kinked vacuum tubing slowly to reach various vacuum rates. Ensure that the level of vacuum is maintains consistency when the vacuum tubing is kinked. Standard Continuous and High Vacuum: Follow the steps below based on mode type 2 Mode: 5. Decrease the vacuum to zero and move the selector switch to the “OFF” position. 3 Mode: 5. Move the selector switch to the “FULL” position. Kink the vacuum tubing and ensure that the vacuum gauge is reflecting the maximum suction available. 5b. Move the selector switch to the “REG” position. 5c. Decrease the vacuum to zero and move the selector switch to the “OFF” position. Pediatric & Neonatal Continuous: 6. In the “REG” position, kink the vacuum tubing and turn the regulator control knob fully in the clockwise direction to ensure that the vacuum level does not go over -21 kPa (-160 mmHg) for Pediatric and -13 kPa (-100mmHg) for Neonatal. 5

NOTE:

This feature is only present in the Pediatric and Neonatal models.

7. Decrease the vacuum level to zero and move the selector switch to the “OFF” position. Always verify vacuum setting prior to performing any procedure.

! WARNING: CAUTION:

When the collection canister is full DO NOT operate the Vacuum Regulator. The WARRANTY WILL BE VOIDED if the canister overflows and contaminates the Vacuum Regulator.

Setup for Patient use: Setting the Level of Vacuum for Patient use: 1. Amvex recommends that the Procedures Prior to Use List be completed. 2 Move the selector switch to the “REG” position. 3. Kink the vacuum tubing. 4. Set the required vacuum level.

! WARNING:

The vacuum tubing must be kinked to ensure that the patient is not exposed to a higher level of vacuum than required.

5. Move the selector switch to the “OFF” position. 6. Attach the vacuum tubing to the vacuum canister.

Cleaning Instructions 1. Connect the supply port of the Vacuum Regulator to the patient port of a collection canister. 2. Attach the vacuum port of the collection canister to a vacuum source. 3. Connect a hose from the patient port of the Regulator to be cleaned and place the other end into a container containing 100cc of a cold sterilant. 4. Fully increase the regulating knob of the vacuum regulator (clockwise). 5. Turn on the Vacuum Regulator to the “REG” mode. Wait until all of the cold sterilant is passed through the regulator. 6. Repeat steps 3,4 & 5 for all modes of the Vacuum Regulator. 7. Repeat steps 3,4 & 5 using 100cc of isopropyl alcohol to purge the Vacuum Regulator of the sterilant. 8. The Regulator should run for 30 sec. in each mode with its patient port open to atmosphere to dry internal parts. CAUTION: Ethylene oxide is not recommended. Sterilization using an ethylene mixture may cause small surface cracks to some of the plastic parts. CAUTION: Do not steam autoclave, immerse in liquid or gas sterilize the Vacuum Regulators. This may damage the unit. CAUTION:

If Vacuum Regulator becomes contaminated internally, warranty is voided. 6

Do not send Vacuum Regulator back to the manufacturer. Follow your facility’s procedures for handling contaminated products. -ODE3ELECTOR3WITCH Mode Selector

Switch

3UPPLY0ORT Supply Port G+NOB

To Vacuum Source

Regulating Knob 0ATIENT0ORT Patient Port

WITH COLD STERILANT OR ALCOHOL Container#ONTAINER with cold sterilizer or alcohol

Recommended Maintenance The following are recommended maintenance steps that should be taken after each patient: 1. Clean the exterior of the Vacuum Regulator with a solution of a diluted mild detergent. 2. Make sure all secondary apparatus such as canisters and tubing are thoroughly cleaned. 3. Inspect the bacteria filter. If it has been contaminated replace with a new one. 4. Inspect the overflow safety trap to make sure it is free of any restrictions.

Replacement Parts VR-AG-100MM-WL

Analog Gauge with Lens 100mmHg

VR-AG-160MM-WL

Analog Gauge with Lens 160mmHg

VR-AG-200MM-WL

Analog Gauge with Lens 200mmHg

VR-AG-300MM-WL

Analog Gauge with Lens 300mmHg

VR-AG-760MM-WL

Analog Gauge with Lens 760mmHg

VR-DG-100MM

Digital Gauge with Lens 100mmHg

VR-DG-160MM

Digital Gauge with Lens 160mmHg

VR-DG-200MM

Digital Gauge with Lens 200mmHg

VR-DG-300MM

Digital Gauge with Lens 300mmHg

VR-DG-760MM

Digital Gauge with Lens 760mmHg

VR-MODULE VR-MODULE-H

Regulating Module Assembly Regulating Module Assembly 760mmHg

VR-ORING-KIT-P

1 Set of O-rings, Gaskets and Filters for all Continuous Pediatric & Neonatal Models.

VR-ORING-KIT-C3

1 Set of O-rings, Gaskets and Filters for all Continuous Models (C3, C2 & CH)

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WARRANTY This Product is sold by Amvex Corp., a Delaware corporation (the “Company”) under the express terms of the warranty set forth below. For a period of THIRTY SIX (36) MONTHS (or for a period of ONE HUNDRED AND TWENTY (120) MONTHS in North America ONLY) from the date the Company ships this Product to the customer, but in no event for a period of more than three years from the date of original delivery by the Company to an authorized dealer, this Product, other than its expendable parts (e.g., batteries for Digital Gauge) is warranted to be free from functional defects in materials and workmanship and to conform in all material respects to the description for the Product contained in this operation manual, if this Product is properly operated under conditions of normal use, regular periodic maintenance and service is performed and repairs are made in accordance with this operation manual. The warranty period for all expendable parts of the Product is sixty (60) days from the date the Company ships the Product to the customer. The foregoing warranty shall not apply if the Product has been repaired or altered by anyone other than the Company or an authorized dealer; or if the Product has been subjected to abuse, misuse, negligence, or accident. The Company reserves the right to stop manufacturing any product or change materials, designs, or specifications without notice. This warranty is extended to only the initial customer with respect to the purchase of this Product directly from the Company or an authorized dealer as new merchandise. Dealers are not authorized to alter or amend the warranty of any Product described in this agreement. Any statements, whether written or oral, will not be honored or be made part of the agreement of sale. THIS WARRANTY IS EXPRESSLY IN LIEU OF ANY OTHER WARRANTIES, EXPRESS OR IMPLIED, INCLUDING ANY WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. THE COMPANY SHALL NOT BE LIABLE FOR INCIDENTAL, COLLATERAL, CONSEQUENTIAL, OR SPECIAL DAMAGES INCLUDING, BUT NOT LIMITED TO, LOST PROFITS, OR LOSS OF USE. THE COMPANY’S LIABILITY, IN THE AGGREGATE, SHALL NOT EXCEED THE PURCHASE PRICE OF THE PRODUCT. In order to file a warranty claim, customer is required to return Product prepaid to the Company at 25B East Pearce Street, Richmond Hill Ontario, L4B2M9 Canada. As determined at the sole discretion of the Company, Products which qualify under the warranty will be repaired or replaced, at the Company’s option, and returned to customer via ground delivery at the Company’s expense. All claims for warranty must first be approved by Amvex Corporations Customer Service Department: (customerservice@ amvex.com or 866-462-6839/905-764-7736). Upon approval the customer service department will issue a Return Goods Authorization (RGA) number. An RGA must be obtained prior to commencement of any warranty claim. Form No. 55024 (Rev.1) 2012 / Form No. 55021 (Rev.1) 2012

© 2014 Ohio Medical Corporation. This document contains information that is proprietary and confidential to Ohio Medical Corporation. Use of this information is under license from Ohio Medical Corporation. Any use other than that authorized by Ohio Medical Corporation is prohibited. Ohio Medical Corporation, the Ohio Medical logo, Amvex and the Amvex logo are registered trademarks of Ohio Medical Corporation. NFPA is a registered trademark of National Fire Protection Association Inc.

Authorized Representative in the European Union:

EC REP

Oxygen Care Ltd. 2 Holfeld Business Park Kilmacanogue Co Wicklow Ireland

VR-C-MANUAL 03/14 8